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Discordant associations of educational attainment with ASD and ADHD implicate a polygenic form of pleiotropy
Autism Spectrum Disorder (ASD) and Attention-Deficit/Hyperactivity Disorder (ADHD) are complex co-occurring neurodevelopmental conditions. Their genetic architectures reveal striking similarities but also differences, including strong, discordant polygenic associations with educational attainment (E...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8586371/ https://www.ncbi.nlm.nih.gov/pubmed/34764245 http://dx.doi.org/10.1038/s41467-021-26755-1 |
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author | Verhoef, Ellen Grove, Jakob Shapland, Chin Yang Demontis, Ditte Burgess, Stephen Rai, Dheeraj Børglum, Anders D. St Pourcain, Beate |
author_facet | Verhoef, Ellen Grove, Jakob Shapland, Chin Yang Demontis, Ditte Burgess, Stephen Rai, Dheeraj Børglum, Anders D. St Pourcain, Beate |
author_sort | Verhoef, Ellen |
collection | PubMed |
description | Autism Spectrum Disorder (ASD) and Attention-Deficit/Hyperactivity Disorder (ADHD) are complex co-occurring neurodevelopmental conditions. Their genetic architectures reveal striking similarities but also differences, including strong, discordant polygenic associations with educational attainment (EA). To study genetic mechanisms that present as ASD-related positive and ADHD-related negative genetic correlations with EA, we carry out multivariable regression analyses using genome-wide summary statistics (N = 10,610–766,345). Our results show that EA-related genetic variation is shared across ASD and ADHD architectures, involving identical marker alleles. However, the polygenic association profile with EA, across shared marker alleles, is discordant for ASD versus ADHD risk, indicating independent effects. At the single-variant level, our results suggest either biological pleiotropy or co-localisation of different risk variants, implicating MIR19A/19B microRNA mechanisms. At the polygenic level, they point to a polygenic form of pleiotropy that contributes to the detectable genome-wide correlation between ASD and ADHD and is consistent with effect cancellation across EA-related regions. |
format | Online Article Text |
id | pubmed-8586371 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85863712021-11-15 Discordant associations of educational attainment with ASD and ADHD implicate a polygenic form of pleiotropy Verhoef, Ellen Grove, Jakob Shapland, Chin Yang Demontis, Ditte Burgess, Stephen Rai, Dheeraj Børglum, Anders D. St Pourcain, Beate Nat Commun Article Autism Spectrum Disorder (ASD) and Attention-Deficit/Hyperactivity Disorder (ADHD) are complex co-occurring neurodevelopmental conditions. Their genetic architectures reveal striking similarities but also differences, including strong, discordant polygenic associations with educational attainment (EA). To study genetic mechanisms that present as ASD-related positive and ADHD-related negative genetic correlations with EA, we carry out multivariable regression analyses using genome-wide summary statistics (N = 10,610–766,345). Our results show that EA-related genetic variation is shared across ASD and ADHD architectures, involving identical marker alleles. However, the polygenic association profile with EA, across shared marker alleles, is discordant for ASD versus ADHD risk, indicating independent effects. At the single-variant level, our results suggest either biological pleiotropy or co-localisation of different risk variants, implicating MIR19A/19B microRNA mechanisms. At the polygenic level, they point to a polygenic form of pleiotropy that contributes to the detectable genome-wide correlation between ASD and ADHD and is consistent with effect cancellation across EA-related regions. Nature Publishing Group UK 2021-11-11 /pmc/articles/PMC8586371/ /pubmed/34764245 http://dx.doi.org/10.1038/s41467-021-26755-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Verhoef, Ellen Grove, Jakob Shapland, Chin Yang Demontis, Ditte Burgess, Stephen Rai, Dheeraj Børglum, Anders D. St Pourcain, Beate Discordant associations of educational attainment with ASD and ADHD implicate a polygenic form of pleiotropy |
title | Discordant associations of educational attainment with ASD and ADHD implicate a polygenic form of pleiotropy |
title_full | Discordant associations of educational attainment with ASD and ADHD implicate a polygenic form of pleiotropy |
title_fullStr | Discordant associations of educational attainment with ASD and ADHD implicate a polygenic form of pleiotropy |
title_full_unstemmed | Discordant associations of educational attainment with ASD and ADHD implicate a polygenic form of pleiotropy |
title_short | Discordant associations of educational attainment with ASD and ADHD implicate a polygenic form of pleiotropy |
title_sort | discordant associations of educational attainment with asd and adhd implicate a polygenic form of pleiotropy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8586371/ https://www.ncbi.nlm.nih.gov/pubmed/34764245 http://dx.doi.org/10.1038/s41467-021-26755-1 |
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